24.04.24 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means - Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents - Interaction with regulatory agencies - Co
Später ansehen02.04.24 | Vollzeit | Ludwigshafen am Rhein | XylemAll project phases (initialization, analysis, concept development, project implementation until handover to accountable organizations). Drive project teams and organizations to comprehensively improve operating model design, process simplification, data & technology enablement, and financial success
Später ansehen24.04.24 | Teilzeit, Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGAnd eye care - and products and services in our Allergan Aesthetics portfolio. Further develop your expertise and join our team as Manager Statistics (all genders) (permanent - full or part time) Job description As part of our Research and Development team, you will be contributing to finding solutions
Später ansehen24.04.24 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means - Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents - Interaction with regulatory agencies - Co
Später ansehen09.04.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen09.04.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen09.04.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen09.04.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen09.04.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
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